Experienced Site Contract Specialist

Medpace; Buenos Aires; Presencial; ARS 106.678.000 - 167.637.000; Jornada completa

Descripción de la vacante

Medpace is seeking a full-time Contract Specialist to join the LatAm Site Contract Team within Clinical Operations. The role focuses on study start-up and management of site contracts with investigators and internal teams.

You will prepare, negotiate and finalize CDA/CTA documents, budgets and LOI amendments, monitor timelines, and mitigate risks to ensure delivery of study milestones and client expectations.

Formación

• Experience negotiating site contracts with investigators or CROs.
• Ability to manage high-volume work and meet strict deadlines.
• Strong communication with internal and external stakeholders.

Responsabilidades

• Prepare, negotiate, track and finalize CDA, CTA, budgets, and LOIs and amendments as needed.
• 2-4 years of site contract negotiation experience preferred.
• Manage all required contractual agreements with investigator sites and track status.

Conocimientos

Contract negotiation

CDA/CTA

Budget negotiation

LOI

Amendments

Site contracts

English fluency

Portuguese desirable

Educación

Bachelor's degree

Descripción del empleo

Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Contract Specialist to join our LatAm Site Contract Team within the Clinical Operations team. This position will report to the LatAm Contract Manager and will play a key role in the study start-up and clinical trial management processes at Medpace. The Contract Specialist will play a key role in advancing the start-up of our projects. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

• Is responsible for preparing, negotiating, tracking and finalizing the Confidentiality Agreements (CDA), Clinical Trial Agreements (CTA), Budgets and Letters of Indemnification (LOI) as well as Amendments to these documents, as needed.
• 2-4 years of site contract negotiation experience preferred.
• Manages all required contractual agreements with investigator sites. This includes distribution, negotiation of budget and language, tracking and finalization.
• Proactively identifies site contract related risks and potential roadblocks.
• Prepares contract approval timelines with investigators and leads efforts to obtain contract approval to meet study deliverables
• Maintains communication with project team and sites regarding status of all contractual requirements
• Collaborates with the project team to ensure the client deliverables and expectations are achieved.
• Liaises with internal customers to review contract or budget areas that impact final execution of site contracts.
• Maintains tracking regarding site contracts and provides regular updates as agreed by the study team to the project team and client regarding status and efforts to ensure timelines are maintained.

Qualifications

• Bachelor’s degree in business administration, legal studies, or life sciences.
• Ability to work with internal and external customers/vendors to meet project-specific goal.
• Ability to manage high volume work and meet rigorous deadlines
• Flexibility to strategically manage negotiations with minimal oversight
• Ability to interact with site and other functional areas as secondary project contact for contracting issues and question.
• Ability to manage time and project requirements based on study deliverables.
• CRO experience or investigator site experience negotiating site agreements preferred.
• Fluency in English. Portuguese desirable.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

• Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

• Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
• Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

• Office based environment with on-site mentors
• Defined career paths with clear advancement opportunities
• Industry renowned onboarding and training programs designed to accelerate professional development
• Ongoing training and continuous learning opportunities throughout your career
• An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

• Competitive compensation programs that recognize and reward performance
• Comprehensive health, wellness, retirement, and PTO benefits
• Office based culture with occasional WFH that provides flexibility for eligible positions after training
• Company-sponsored social events

Please note benefits may vary based on country.

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview.

While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.